Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43389763-43389955 | Common:3; Rare:85 | ||||
chr1:43946629-43946987 | Rare:96 | ||||
chr1:44674401-44674756 | Common:3; Rare:97 | ||||
chr1:44739641-44739941 | Common:3; Rare:124 | ||||
chr1:44775445-44775607 | Rare:61 | ||||
chr1:44986532-44986733 | Common:2; Rare:38; Clinvar (benign):1 | ||||
chr1:45339996-45340212 | Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45500056-45500358 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521833-45522087 | Common:1; Rare:100 | ||||
chr1:45550730-45551112 | Common:3; Rare:93 | ||||
chr1:45583931-45584078 | Rare:57 | ||||
chr1:45687059-45687351 | Common:1; Rare:75 | ||||
chr1:45688059-45688211 | Common:1; Rare:39 | ||||
chr1:45750618-45750793 | Rare:66 | ||||
chr1:46132622-46132774 | Rare:54 |